Difference between revisions of "Part:BBa K2922029"

 
 
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<partinfo>BBa_K2922029 short</partinfo>
 
<partinfo>BBa_K2922029 short</partinfo>
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===Summary===
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Abbreviated as Nkil, lysis protein for Colicin-N is a 5.6 kDa protein, which is encoded by gene <i>cnl</i>. The lysis protein is required for both Colicin-E1 release and partial cell lysis<ref>[1]https://link.springer.com/article/10.1007/BF00330613</ref>. (Fig.1)
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<table><tr><th>[[File:Ndesign.png|thumb|720px|Fig.1 Nkil helps Colicin-N release and makes partial cell lysis.]]</th><th></table>
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===Identification===
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When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit is built, we sent the plasmid to sequence, and got the correct sequencing.
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After new molecular cloning experiments, we did Enzyme-Cut identification to certify the plasmid was correct. We used the <i>Xba</i>I and <i>Pst</i>I to cut the plasmid, then we got the target separate fragment-159bp. (Fig.2)
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<table><tr><th>[[File:Nkil-Ekil.png|thumb|300px|Fig.2 The result of this plasmid cut with enzyme <i>Xba</i>I and <i>Pst</i>I.]]</th><th></table>
  
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Lysis proteins are required for both colicin release and partial cell lysis.
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===Sequence and Features===
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===Usage and Biology===
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K2922029 SequenceAndFeatures</partinfo>
 
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<partinfo>BBa_K2922029 parameters</partinfo>
 
<partinfo>BBa_K2922029 parameters</partinfo>
 
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===Reference===

Latest revision as of 18:00, 20 October 2019


Lysis protein for colicin-N coding region

Summary

Abbreviated as Nkil, lysis protein for Colicin-N is a 5.6 kDa protein, which is encoded by gene cnl. The lysis protein is required for both Colicin-E1 release and partial cell lysis[1]. (Fig.1)

Fig.1 Nkil helps Colicin-N release and makes partial cell lysis.

Identification

When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit is built, we sent the plasmid to sequence, and got the correct sequencing. After new molecular cloning experiments, we did Enzyme-Cut identification to certify the plasmid was correct. We used the XbaI and PstI to cut the plasmid, then we got the target separate fragment-159bp. (Fig.2)

Fig.2 The result of this plasmid cut with enzyme XbaI and PstI.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 118
  • 1000
    COMPATIBLE WITH RFC[1000]


Reference

  1. ↑ [1]https://link.springer.com/article/10.1007/BF00330613